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6-Nitro-1,3-Benzoxazole

    • Product Name 6-Nitro-1,3-Benzoxazole
    • Alias 6-Nitrobenzo[d]oxazole
    • Einecs 629-003-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    745700

    Productname 6-Nitro-1,3-Benzoxazole
    Casnumber 10435-45-1
    Molecularformula C7H4N2O3
    Molecularweight 164.12
    Appearance Yellow to orange crystalline powder
    Meltingpoint 168-172°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥98%
    Storagetemperature Store at room temperature (15-25°C)
    Synonyms 6-Nitrobenzo[d]oxazole
    Smiles c1cc2onc(c2cc1)[N+](=O)[O-]
    Inchi InChI=1S/C7H4N2O3/c10-9(11)6-2-1-5-7(3-6)8-4-12-5/h1-4H

    As an accredited 6-Nitro-1,3-Benzoxazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 6-Nitro-1,3-Benzoxazole (25g) is packaged in a sealed amber glass bottle with tamper-evident cap, labeled for safety.
    Shipping **6-Nitro-1,3-Benzoxazole** is shipped in tightly sealed, labeled containers, protected from light, moisture, and incompatible substances. It is classified as a hazardous chemical, requiring appropriate UN packaging and transport in accordance with international regulations. Ensure shipment includes safety documentation and follows all relevant regulatory and safety guidelines.
    Storage 6-Nitro-1,3-Benzoxazole should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizing or reducing agents. Protect from light and moisture. Clearly label containers and follow all applicable chemical storage regulations and safety guidelines. Store at room temperature unless otherwise specified.
    Application of 6-Nitro-1,3-Benzoxazole

    Applications of 6-Nitro-1,3-Benzoxazole in Industrial Manufacturing

    As an advanced fine chemical manufacturer, we directly supply 6-Nitro-1,3-Benzoxazole to formulation plants and processing companies with proven, industrial-scale adoption in several niche performance chemical sectors. Below, we detail selected application scenarios where our product enters the value chain, with precise data and regulatory references reflecting customers’ real-world use.

    1. Optical Brightener Intermediate for Polyester Fiber Production

    Major manufacturers in the synthetic fiber industry use 6-Nitro-1,3-Benzoxazole as a specialty intermediate for the synthesis of benzoxazole-based optical brighteners, which get incorporated into polyester melt spinning operations to impart enhanced whiteness and UV resistance. Customers adjust the intermediate’s input based on the optical brightener formulation, production lot scale, and brightness requirements dictated by end-customer textile specifications.

    Industry compliance standards

    • OEKO-TEX® Standard 100 chemical restrictions (Annex 4)
    • REACH Regulation (EC) No. 1907/2006 (SVHC and Annex XVII compliance)
    • ZDHC MRSL V3.1 for polymers and textile chemicals
    • ISO 9001:2015 Quality Management for fiber chemical supply

    Typical usage ratio

    • Ranges from 0.1% to 0.5% w/w in optical brightener synthesis batch, adjusted per targeted brightness index
    • Further diluted to 10–200 ppm in polyester dope addition for fiber spinning

    Downstream process integration

    • Condensation stage during optical brightener synthesis in chemical reactors
    • Downstream blending of synthesized brightener into polyester melt before spinning

    Final product types

    • High-brightness polyester filaments and staple fibers
    • Textile-grade chips for spinning mills
    • Ready-to-use masterbatches for optical fiber and film grades

    2. API Intermediate for Third-Generation Quinolone Antibiotics

    Leading pharmaceutical API manufacturers utilize 6-Nitro-1,3-Benzoxazole as a key intermediate in the synthetic route for advanced quinolone antibiotics, particularly in the assembly of core heterocyclic moieties. The integration of our material takes place under GMP-controlled conditions, and its concentration directly influences the final impurity profile and yield of the antibiotic active ingredient.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA CFR Title 21 Part 211 (for cGMP compliance)
    • Ph. Eur. (European Pharmacopoeia) monographs for quinolones
    • Chinese Pharmacopoeia (ChP)

    Typical usage ratio

    • 0.3–0.8 molar equivalents relative to quinolone scaffold precursor
    • Exact ratio depends on process yield optimization and impurity control requirements

    Downstream process integration

    • Enters the cyclization or coupling step in multi-step heterocycle construction under GMP batch synthesis
    • Residual handling and recovery steps employ strict in-process test controls

    Final product types

    • Bulk crystalline quinolone API for formulation
    • Sterile and non-sterile active pharmaceutical ingredients
    • Intermediates for finished dosage form tablets and injectables

    3. UV-Absorber Precursor for Engineering Plastics Compounding

    Manufacturers producing UV-absorber masterbatches for engineering resins such as PC, PET, and PMMA source 6-Nitro-1,3-Benzoxazole as a necessary building block in high-performance benzoxazole UV stabilizer molecules. Consistent purity and assay guarantee predictable additive function, with addition rates dependent on polymer substrate, desired UV cut-off, and outdoor weathering demands.

    Industry compliance standards

    • UL 746C and UL 94 regulations for polymer additives
    • EU Regulation (EU) No. 10/2011 for plastics intended to contact food (for food-contact applications)
    • ISO 4892-2 Xenon Arc Weathering Test requirements
    • RoHS Directive 2011/65/EU (chemical use restrictions)

    Typical usage ratio

    • Starts at 0.05% and can reach up to 1.00% w/w in masterbatch formulation, tailored per substrate and weathering standard
    • Final UV-absorber loading in end-use plastic: typically 200–1000 ppm

    Downstream process integration

    • Chemical synthesis step for benzoxazole UV-absorber compounds
    • Extrusion compounding into polymer matrix as concentrated masterbatch pellets

    Final product types

    • UV-stabilized automotive plastics components
    • Outdoor-rated equipment housings
    • Transparent, UV-resistant electronic enclosures

    4. Analytical Reagent for Fluorescent Sensor Manufacturing

    Producers of chemical sensors and specialized fluorescent dyes employ 6-Nitro-1,3-Benzoxazole as a functional core for molecular probe synthesis. The dosing and purity must meet instrument-grade requirements, and incorporation occurs in designated reagent manufacturing steps to ensure precise photophysical properties tailored for analytical instruments.

    Industry compliance standards

    • ISO/IEC 17025-accredited laboratory chemical standards
    • ASTM E2879-13 (quantification of molecular fluorescence emission)
    • National Metrology Institute purity requirements (as applicable)
    • Cleanroom ISO 14644-1 conditions for analytical reagent mixing

    Typical usage ratio

    • Input is calibrated from 0.01 mmol to 0.2 mmol per reagent batch, based on probe molecule design
    • Adjusted for desired fluorescence wavelength and sensitivity range

    Downstream process integration

    • Introduced during condensation or cyclization steps in fluorophore assembly
    • Post-synthesis purification under trace-metal-free conditions

    Final product types

    • Fluorescent probes for laboratory analysis
    • Chemical sensor kits for industrial and environmental applications
    • Instrument calibration standards
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    Certification & Compliance
    More Introduction

    6-Nitro-1,3-Benzoxazole: Shaping Performance from the Lab Floor

    A Look Inside Our Manufacturing Experience

    The story of 6-Nitro-1,3-Benzoxazole begins long before a customer opens a drum or a flask. Sourcing quality raw materials stands as the first line of impact. We have spent years developing reliable channels for secure, compliant supply of benzoxazole intermediates, and this investment in supply chain control keeps batch quality tight and fluctuations rare. Our team handles every nitro group addition in-house, giving us an edge that runs deeper than surface-level claims of quality control. 

    Pinpointing Our Product: Molecular Sharpening and Selective Stability

    6-Nitro-1,3-Benzoxazole, chemical formula C7H4N2O3, shows up as a pale yellow solid beneath the glass. Over the last decade, we have calibrated the nitro group introduction to steer clear of over-oxidation and byproduct entrapment. Product purity consistently crosses the 99% mark, especially in our high-spec model 6NBO-99. The particulate profile stands out: median diameter falls in the lower micron range, reducing issues with caking or dissolution lag in downstream use. 

    We found that the smallest shift in moisture during storage, even half a percent, affects flow performance once you move from kilo to ton batches. After a few experiences where minor clumping forced customers to stop their lines, we updated our drying and nitrogen-purged packaging protocols. Every batch is tested for thermal stability, which, years ago, meant chasing exotherms across the DSC screen with every change in raw component. Today, the product easily tolerates handling temperatures commonly encountered in scale-up reactors without risk of runaway decomposition.

    Application Backbone: What Sets This Nitrobenzoxazole Apart

    Much of 6-Nitro-1,3-Benzoxazole’s value comes from its use as a building block in pharmaceutical and specialty material synthesis. On the API side, researchers lean on it for constructing benzoxazole-linked biologically active compounds, such as antimicrobial and anti-inflammatory agents. The electronic materials crowd demands it for its strong electron-withdrawing effect, tuning the reactivity of larger heterocyclic scaffolds. You will see it at the start of new molecule development—its nitro group both activates the ring for nucleophilic attack and serves as a handy anchor for further transformation. 

    In the mid-2010s, our customers pushed into more complex structures for OLED and battery electrolytes. The consistent performance of our 6-Nitro-1,3-Benzoxazole allowed them to run larger, more temperature-sensitive reactions without excess cleanup or purity drift. Keeping side-products below 0.3% cut down on column runs and solvent waste—a small number that becomes significant at pilot and commercial scale.

    From Batch to Bulk: How Reproducibility Drives Value

    The biggest challenge we see in heterocyclic manufacturing is loss of reproducibility across lots. Tiny differences in particle size or residual moisture sometimes translate to tens of hours in lost reactor operation, especially during sensitive coupling or reduction steps. By tightening controls on both the nitration and purification process, we build reliability batch after batch. 

    Our best model, 6NBO-99, undergoes extended thermal cycling and impurity sweep testing before packing. We also run a secondary screening for transition metal content, informed by cases from the solar cell material sector where even trace levels disrupted device performance. As manufacturers, we understand that once our product enters a partner’s system—be it pharmaceutical synthesis or materials fabrication—there’s no room for last-minute surprises or unknowns.

    Pain Points in Manufacturing and User Experience: Facing Real-World Hurdles

    Producing 6-Nitro-1,3-Benzoxazole at scale brings its own technical headaches. The nitration of 1,3-benzoxazole must balance reactivity to land the nitro group at the six-position without runaway side-reactions. Minor shifts in batch temperature, and even mixing rates, can skew substitution away from the target position. A decade ago, we lost a week’s production to an unexpected spike in dinitro byproduct. Learning from those days, process control for us now runs as a human-and-machine partnership, never just automated sensors.

    Another challenge is the removal of mineral acid traces after reaction. Most downstream users—especially those in the API and dye sectors—have strict acid and heavy metal limits, both for regulatory and performance reasons. We engineer rinsing and neutralization steps into every lot, and we validate these through titration and surface analysis. The cost of such diligence shows up in lower—but less variable—yields, which in the end is a trade-off most of our users appreciate.

    Listening and Solving: End-Use Demands Shape Our Offerings

    Customers in specialty chemicals keep us on our toes with requests tailored to their lines. We frequently tweak particle size and drying levels to match user setups, especially continuous slurry or high-throughput reactors. Some polymer additive producers request 6-Nitro-1,3-Benzoxazole free-flowing at 25 kg scale, not just 1 kg samples. This feedback loop propels us to refine granulation and anti-caking strategies further—a process that, for us, spans lab to shipping dock.

    On the safety front, we pay attention to concerns about dust inhalation and handling volatility. While the compound poses lower vapor risk than many aromatic nitro derivatives, its fine powder can pose respiratory hazards if mishandled. Over the last five years, we have improved dust minimization both during packaging and in transfer by switching to double-layered liners and pneumatic fill systems. Findings from our incident logs—cases of minor skin or eye irritation—have driven us to engineer only tightly sealed, easy-to-open packs.

    Comparison with Related Benzoxazole Products

    To understand the strengths of 6-Nitro-1,3-Benzoxazole, it helps to look at close structural relatives, such as 2-Nitro-1,3-Benzoxazole or unsubstituted benzoxazoles. Unlike the two-position isomer—which steers reactivity in a different direction during cross-coupling—the six-position nitro compound offers a reliable route for further substitution at the ortho and para positions of the benzo ring. Our experience shows that using six-position products reduces side-reaction risk during azo coupling and other nucleophilic substitutions. 

    Comparing with chlorinated benzoxazole intermediates, such as 6-chloro-1,3-benzoxazole, the nitro version opens possibilities for downstream reduction to amines and other transformations, supporting diverse synthetic pathways. Reduction of the nitro group can proceed under milder conditions than comparable halo-compounds, reducing corrosion in standard glass-lined reactors and trimming the need for aggressive dehydrohalogenation steps. Feedback from pharma customers shows fewer issues with catalyst poisoning or halide buildup when switching from chloro to nitro intermediates, which echoes our own internal batch testing.

    Our products differ from off-the-shelf solutions in moisture control and trace metal detection. By combining Karl Fischer moisture checks with ICP-OES analysis for transition metals in every batch, we spot out-of-spec issues earlier. This workflow helps those scaling up for new product launches avoid requalification—a process that can cost months and jeopardize compliance schedules.

    Sustainability and Compliance: Manufacturing with Foresight

    Our team has adjusted production to align with stricter waste control and safer chemical management standards, both internationally and domestically. This move grew from necessity: traditional nitration routes generate substantial acidic effluents requiring careful neutralization before discharge. Several years back, we pivoted to a closed-loop acid recovery system, significantly lowering the water and chemical footprint per kilogram produced. 

    We also work closely with specialty disposal partners for any out-of-spec or off-grade material, converting would-be waste into lower-tier intermediates for other sectors. Reducing the frequency and volume of non-compliant lots means fewer interruptions for everyone in the chain, and supports both our long-term relationships and regulatory standing.

    Bridging Research and Production: Supporting the Next Innovation Wave

    Academic and industrial R&D teams rely on timely, consistent supply of specialty reagents. Limited availability and inconsistent quality in the early days held back innovation in benzoxazole chemistry—we know because our founders struggled with it in their own postdoc years. By keeping production in-house and being able to scale from gram to multi-tonne quantities with the same baseline specifications, we remove several bottlenecks for discovery and pilot teams. 

    Startup biotech groups and established chemical giants benefit from this approach. Over and over, we hear that the transition from benchtop discovery to pilot reactors stumbles on product inconsistency or shifting impurity profiles. By supporting researchers not just with samples, but by involving them in setting specifications and troubleshooting process hiccups together, we enable more compounds to leave the proof-of-concept phase behind.

    Handling and Storage Advice: Sharing What Works

    A product’s shelf life depends on packaging, not just purity at production. We advise storing 6-Nitro-1,3-Benzoxazole inside dry, well-sealed containers away from direct heat sources or oxidizing agents. Based on requests from the fine chemical sector, we switched years ago to multi-layer PTFE-lined drums that permit resealing after partial use. Customers regularly report two-year viability under otherwise ordinary ambient conditions.

    Every now and then, we notice a customer suffers product degradation due to humidity leakage; to help stem this, we now pack smaller, single-use sachets for R&D-scale use. Our goal remains to keep the material as reliable as it is freshly packed, no matter the project timeline.

    Driving Continuous Improvement through Partnership

    Some properties of 6-Nitro-1,3-Benzoxazole never turn up in glossy brochures. Real-world reactor loads, long storage, outlier environmental shifts—all impact performance. Over the years, we have learned much from customer troubleshooting. In one case, a material developer for next-generation display panels found batch-to-batch color differences. Working jointly, we traced this to a minor, previously unmonitored trace impurity, leading us to add an extra HPLC check mid-production. Small changes like these—originating in real user experience—end up benefiting every order shipped.

    We pay close attention to emerging regulatory trends and market priorities, understanding that what counts as impurity limit or safety precaution today will keep rising year after year. Keeping pace with these upward shifts requires both investment in analytical technology and commitment to open dialogue with users and regulators alike.

    Summing Up: Why Our Manufacturing Approach Matters

    Supplying 6-Nitro-1,3-Benzoxazole in a dependable, tailored format reflects more than just technical ability. Every improvement and adaptation—whether prompted by a persistent flow issue, an unplanned shutdown, or a change in local safety code—grows from hands-on experience. We continue to see value not only in producing a reliable chemical, but in making the day-to-day work easier for those transforming it into next-generation drugs, advanced materials, and specialty products. As new uses and higher standards emerge, we remain committed to grounding our process in both robust science and attentive, practical know-how honed over decades in chemical manufacturing.